HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558460Generated: October 25, 2026
Water → 2-(4-Methoxybenzyloxy)-3-bromo-4-methylpyridine
https://huagongshe.com/reaction/558460
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methoxybenzyl alcohol | HCID 7738 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Bromo-2-chloro-4-methylpyridine | HCID 40425119 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Methoxybenzyloxy)-3-bromo-4-methylpyridine | HCID 67000104 | — |
Reaction Steps
To a mixture of 60% NaH in mineral oil (0.290 g, 7.27 mmol) in THF (15 mL) at RT in a resealable pressure vessel was added (4-methoxyphenyl)methanol (0.906 ml, 7.27 mmol). After 5 minutes, 3-bromo-2-chloro-4-picoline (1.00 g, 4.84 mmol) was added and the mixture was heated to 75° C. After 1 hr, water was added and the mixture was diluted with EtOAc. After washing with water and brine, the organic fraction was dried with sodium sulfate and purified by silica gel chromatography using 0-30% EtOAc:hexanes to afford 2-(4-methoxybenzyloxy)-3-bromo-4-methylpyridine as a colorless oil. M+H+=308.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063055B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-00729da3fd854147b1d35bcb61d2fdee |
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| Source note | uspto-grants-2011_11 |
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